Variant report

Variant	nsv608159
Chromosome Location	chr7:110851553-111169227
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2448)
CpG islands
(count:305)
Chromatin interactive
region (count:256)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2448 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:110968691-110969273	K562	blood:	n/a	n/a
2	ARID3A	chr7:111150377-111150555	K562	blood:	n/a	n/a
3	ARID3A	chr7:110869353-110869485	K562	blood:	n/a	n/a
4	ARID3A	chr7:110966486-110967469	K562	blood:	n/a	n/a
5	ARID3A	chr7:110969611-110970170	K562	blood:	n/a	n/a
6	ARID3A	chr7:111118669-111118974	K562	blood:	n/a	n/a
7	ARID3A	chr7:111024781-111024793	K562	blood:	n/a	n/a
8	ARID3A	chr7:111099362-111100398	K562	blood:	n/a	n/a
9	ARID3A	chr7:111100636-111100911	K562	blood:	n/a	chr7:111100841-111100857
10	ARID3A	chr7:111077670-111079453	K562	blood:	n/a	chr7:111078420-111078436 chr7:111078560-111078576
11	ARID3A	chr7:110968080-110968421	K562	blood:	n/a	n/a
12	ARID3A	chr7:111126348-111127214	K562	blood:	n/a	n/a
13	ARID3A	chr7:111116731-111117824	K562	blood:	n/a	n/a
14	ARID3A	chr7:110967767-110967878	K562	blood:	n/a	n/a
15	ARID3A	chr7:110946747-110946768	K562	blood:	n/a	n/a
16	ARID3A	chr7:111064774-111065198	HepG2	liver:	n/a	n/a
17	ARID3A	chr7:110953154-110953413	K562	blood:	n/a	n/a
18	ARID3A	chr7:110863537-110864343	K562	blood:	n/a	chr7:110863547-110863563 chr7:110863548-110863564
19	ARID3A	chr7:110997534-110997571	K562	blood:	n/a	n/a
20	ARID3A	chr7:110895612-110896118	K562	blood:	n/a	n/a
21	ARID3A	chr7:111126639-111126960	HepG2	liver:	n/a	n/a
22	ARID3A	chr7:111008626-111008764	K562	blood:	n/a	n/a
23	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
24	ARID3A	chr7:111021038-111021344	HepG2	liver:	n/a	n/a
25	ARID3A	chr7:111114444-111116392	K562	blood:	n/a	chr7:111115784-111115800 chr7:111114896-111114912 chr7:111114897-111114913
26	ATF1	chr7:111078600-111078973	K562	blood:	n/a	n/a
27	ATF1	chr7:111115090-111115592	K562	blood:	n/a	n/a
28	ATF1	chr7:111116070-111116343	K562	blood:	n/a	n/a
29	ATF1	chr7:111163232-111163327	K562	blood:	n/a	n/a
30	ATF1	chr7:110863987-110864363	K562	blood:	n/a	n/a
31	ATF1	chr7:110889894-110890092	K562	blood:	n/a	n/a
32	ATF1	chr7:111139180-111139448	K562	blood:	n/a	n/a
33	ATF1	chr7:111054516-111054769	K562	blood:	n/a	n/a
34	ATF1	chr7:111012802-111012930	K562	blood:	n/a	n/a
35	ATF1	chr7:110895660-110895855	K562	blood:	n/a	n/a
36	ATF1	chr7:111126656-111126990	K562	blood:	n/a	n/a
37	ATF2	chr7:111167522-111167997	GM12878	blood:	n/a	n/a
38	ATF2	chr7:111053704-111054218	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF2	chr7:111167450-111168045	GM12878	blood:	n/a	n/a
40	ATF3	chr7:111078506-111078989	K562	blood:	n/a	n/a
41	ATF3	chr7:111156585-111157142	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915
42	ATF3	chr7:111116052-111116358	K562	blood:	n/a	n/a
43	ATF3	chr7:111156586-111157138	A549	lung:	n/a	chr7:111156907-111156914 chr7:111156904-111156914 chr7:111156906-111156917 chr7:111156906-111156920 chr7:111156904-111156917 chr7:111156904-111156915
44	ATF3	chr7:111138942-111139670	A549	lung:	n/a	n/a
45	ATF3	chr7:111138963-111139597	A549	lung:	n/a	n/a
46	ATF3	chr7:110872430-110873085	A549	lung:	n/a	n/a
47	BACH1	chr7:111160755-111160869	K562	blood:	n/a	n/a
48	BACH1	chr7:110935269-110935465	K562	blood:	n/a	n/a
49	BACH1	chr7:110864793-110865013	K562	blood:	n/a	n/a
50	BATF	chr7:111029015-111029334	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110879415-110879465	HAEpiC	amniotic membrane:	n/a
2	chr7:111033064-111033114	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:110879415-110879465	GM19239	blood:	n/a
4	chr7:111033064-111033114	AG04450	lung:	fetal
5	chr7:110906785-110906835	HNPCEpiC	eye:	n/a
6	chr7:110879415-110879465	PANC-1	pancreas:	n/a
7	chr7:111086055-111086105	Hepatocyte	liver:	n/a
8	chr7:111079100-111079150	MCF-7	breast:	n/a
9	chr7:111033064-111033114	GM06990	blood:	n/a
10	chr7:111086055-111086105	GM12878	blood:	n/a
11	chr7:111033064-111033114	HCM	heart:	n/a
12	chr7:110906785-110906835	Hela-S3	cervix:	n/a
13	chr7:111079100-111079150	Caco-2	colon:	n/a
14	chr7:111033064-111033114	H1-hESC	embryonic stem cell:	embryo
15	chr7:111079100-111079150	K562	blood:	n/a
16	chr7:111033064-111033114	HRCEpiC	kidney:	n/a
17	chr7:110879415-110879465	HL-60	blood:	n/a
18	chr7:111079100-111079150	AG04449	skin:	fetal
19	chr7:111086055-111086105	GM06990	blood:	n/a
20	chr7:111079100-111079150	SK-N-SH_RA	brain:	n/a
21	chr7:110906785-110906835	K562	blood:	n/a
22	chr7:110879415-110879465	ovcar-3	ovarian:	n/a
23	chr7:110879415-110879465	AG09319	gingival:	n/a
24	chr7:111033064-111033114	Hepatocyte	liver:	n/a
25	chr7:110906785-110906835	IMR90	lung:	fetal
26	chr7:110879415-110879465	U87	brain:	n/a
27	chr7:111033064-111033114	GM12892	blood:	n/a
28	chr7:110906785-110906835	HIPEpiC	eye:	n/a
29	chr7:111086055-111086105	PrEC	prostate:	n/a
30	chr7:111086055-111086105	MCF-7	breast:	n/a
31	chr7:111079100-111079150	AG09319	gingival:	n/a
32	chr7:111079100-111079150	GM12892	blood:	n/a
33	chr7:111033064-111033114	LNCaP	prostate:	n/a
34	chr7:110879415-110879465	RPTEC	kidney:	n/a
35	chr7:110906785-110906835	HEK293	kidney:	embryo
36	chr7:110906785-110906835	BE2_C	brain:	n/a
37	chr7:111033064-111033114	Caco-2	colon:	n/a
38	chr7:111086055-111086105	H1-hESC	embryonic stem cell:	embryo
39	chr7:111079100-111079150	NHBE	bronchial:	n/a
40	chr7:110879415-110879465	AG04450	lung:	fetal
41	chr7:111079100-111079150	Jurkat	blood:	n/a
42	chr7:110906785-110906835	GM06990	blood:	n/a
43	chr7:111086055-111086105	SK-N-SH_RA	brain:	n/a
44	chr7:111079100-111079150	PrEC	prostate:	n/a
45	chr7:111033064-111033114	HMEC	breast:	n/a
46	chr7:110906785-110906835	SKMC	muscle:	n/a
47	chr7:111079100-111079150	PFSK-1	brain:	n/a
48	chr7:111086055-111086105	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:111033064-111033114	BE2_C	brain:	n/a
50	chr7:110879415-110879465	Hela-S3	cervix:	n/a

(count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr7:110955341..110956918-chr7:110957234..110959729,2	K562	blood:
2	chr7:110846405..110848807-chr7:110859320..110861910,2	K562	blood:
3	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:
4	chr7:110850499..110852525-chr7:110861582..110863250,2	K562	blood:
5	chr7:111099278..111101723-chr7:111102972..111106150,5	K562	blood:
6	chr7:111134697..111137160-chr7:111200355..111203674,3	K562	blood:
7	chr7:110867615..110869914-chr7:110870998..110874841,5	K562	blood:
8	chr7:110864193..110867019-chr7:110872692..110875184,2	K562	blood:
9	chr7:111123975..111126506-chr7:111135381..111138359,2	K562	blood:
10	chr7:111027546..111029195-chr7:111032815..111035330,2	K562	blood:
11	chr7:111149350..111150943-chr7:111156315..111157965,2	K562	blood:
12	chr7:111164149..111167742-chr7:111173784..111176807,4	K562	blood:
13	chr7:111079252..111081356-chr7:111081507..111084110,2	K562	blood:
14	chr7:110997175..111000339-chr7:111001551..111003490,3	K562	blood:
15	chr17:41463788..41465299-chr7:111034758..111036259,2	K562	blood:
16	chr7:110969503..110970311-chr7:111375483..111376413,3	K562	blood:
17	chr7:110843078..110846205-chr7:110849161..110854141,4	K562	blood:
18	chr7:110962569..110964668-chr7:110968085..110971412,3	K562	blood:
19	chr12:108202177..108204461-chr7:111052206..111055078,3	MCF-7	breast:
20	chr7:111018295..111020688-chr7:111021531..111024788,3	MCF-7	breast:
21	chr7:111033110..111035570-chr7:111037254..111039437,2	K562	blood:
22	chr7:111138086..111139591-chr7:111219192..111221961,2	MCF-7	breast:
23	chr7:111132543..111134860-chr7:111136175..111139021,3	K562	blood:
24	chr7:110924432..110929578-chr7:110932859..110937635,6	K562	blood:
25	chr7:110876830..110878652-chr7:110880390..110881983,2	K562	blood:
26	chr7:110730888..110731598-chr7:111126458..111127265,2	K562	blood:
27	chr7:110935982..110938365-chr7:110942817..110944691,2	K562	blood:
28	chr7:110969852..110970371-chr7:111126745..111127278,2	K562	blood:
29	chr7:110873178..110876028-chr7:110879023..110881102,2	K562	blood:
30	chr7:110922885..110927148-chr7:110927337..110932171,6	K562	blood:
31	chr7:110901387..110901887-chr9:130159518..130160059,2	Hela-S3	cervix:
32	chr7:110959106..110960834-chr7:110964696..110967313,2	K562	blood:
33	chr7:111164432..111166766-chr7:111167043..111169484,2	MCF-7	breast:
34	chr7:110994535..110996072-chr7:110997457..110999303,2	K562	blood:
35	chr7:110959334..110960882-chr7:110965813..110967484,2	K562	blood:
36	chr7:110975243..110978153-chr7:110979724..110981495,2	K562	blood:
37	chr7:110907955..110909675-chr7:110912861..110914751,2	K562	blood:
38	chr7:110901427..110902958-chr7:110904579..110907166,2	MCF-7	breast:
39	chr7:111030397..111032923-chr7:111067377..111070241,2	K562	blood:
40	chr7:111096109..111097696-chr7:111100341..111102536,2	K562	blood:
41	chr7:111123279..111126052-chr7:111128693..111130965,2	K562	blood:
42	chr7:110922885..110927148-chr7:110927337..110932171,6	K562	blood:
43	chr7:110907955..110909675-chr7:110912861..110914751,2	K562	blood:
44	chr7:111017537..111020347-chr7:111082285..111084321,2	K562	blood:
45	chr7:111025105..111026879-chr7:111027995..111029881,2	K562	blood:
46	chr7:110970635..110973843-chr7:110975141..110978905,5	K562	blood:
47	chr7:111149350..111150943-chr7:111156315..111157965,2	K562	blood:
48	chr7:110867615..110870539-chr7:110870998..110875749,6	K562	blood:
49	chr7:110729634..110730189-chr7:110952732..110953606,2	MCF-7	breast:
50	chr7:111092714..111094433-chr7:111113503..111115872,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK4-7	chr7:110902289-110902553	expReg_chr7_8342_-

No data

Variant related genes	Relation type
ENSG00000227948	TF binding region
IMMP2L	TF binding region
ENSG00000243621	TF binding region
ENSG00000227948	CpG island
IMMP2L	CpG island
ENSG00000243621	CpG island
ENSG00000188825	chromatin interactions
ENSG00000136856	chromatin interactions
ENSG00000227948	chromatin interactions
ENSG00000173114	chromatin interactions
ENSG00000243621	chromatin interactions
ENSG00000184903	chromatin interactions

Extended variants
information (count: 11032 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:11032 , 50 per page) page: 1 2 3 4 5 6 7 ... 221

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs214460	chr7:110851553-110851554	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574559189	chr7:110851570-110851571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554033595	chr7:110851619-110851620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111885046	chr7:110851620-110851621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532060462	chr7:110851623-110851624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545403408	chr7:110851668-110851669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150715143	chr7:110851686-110851687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113877411	chr7:110851774-110851775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557796635	chr7:110851787-110851788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371808537	chr7:110851789-110851790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573568217	chr7:110851793-110851794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368373166	chr7:110851797-110851798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150054532	chr7:110851814-110851815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111900330	chr7:110851831-110851832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs60022617	chr7:110851836-110851837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs550054506	chr7:110851846-110851847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374405407	chr7:110851876-110851877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111740472	chr7:110851925-110851926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555444110	chr7:110851957-110851958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552625293	chr7:110851977-110851978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566056505	chr7:110851989-110851990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376700506	chr7:110852008-110852009	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs534950590	chr7:110852023-110852024	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs192678395	chr7:110852048-110852049	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs183297134	chr7:110852080-110852081	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs537251392	chr7:110852090-110852091	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs556835355	chr7:110852095-110852096	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs111328959	chr7:110852112-110852113	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs186921739	chr7:110852116-110852117	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs371058382	chr7:110852169-110852170	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs531442653	chr7:110852197-110852198	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs386716848	chr7:110852210-110852211	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs547851990	chr7:110852216-110852217	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs142542772	chr7:110852229-110852230	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs545466848	chr7:110852236-110852237	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs545257525	chr7:110852245-110852246	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs187796953	chr7:110852287-110852288	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs572492617	chr7:110852383-110852384	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs562925135	chr7:110852386-110852387	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs541367902	chr7:110852403-110852404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs193164665	chr7:110852437-110852438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs60383797	chr7:110852446-110852447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530283252	chr7:110852447-110852448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573337824	chr7:110852489-110852490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563698189	chr7:110852512-110852513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532680669	chr7:110852538-110852539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574037797	chr7:110852549-110852550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552686966	chr7:110852556-110852557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566119913	chr7:110852685-110852686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535012964	chr7:110852692-110852693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21509527	CNVD
Glioma	20126413	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Autism	20841430	CNVD
Autism	20685689	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1599 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110838800-110864000	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr7:110842600-110852000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr7:110844400-110853000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:110846000-110864000	Weak transcription	Left Ventricle	heart
5	chr7:110848400-110853000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr7:110850000-110851800	Enhancers	Muscle Satellite Cultured Cells	--
7	chr7:110850400-110851800	Enhancers	Osteobl	bone
8	chr7:110850800-110851600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:110850800-110851600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr7:110851000-110851800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:110851000-110851800	Enhancers	HUVEC	blood vessel
12	chr7:110851200-110851600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr7:110851200-110851600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:110851200-110851600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr7:110851200-110851600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr7:110851200-110851600	Enhancers	NH-A	brain
17	chr7:110851600-110854800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr7:110852000-110852400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
19	chr7:110852000-110853000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:110852000-110853400	Weak transcription	Pancreas	Pancrea
21	chr7:110852400-110853000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:110852400-110853200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr7:110852400-110853400	Weak transcription	Fetal Intestine Small	intestine
24	chr7:110852800-110853800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr7:110853000-110853200	Enhancers	Spleen	Spleen
26	chr7:110853000-110853400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:110853000-110853600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr7:110853000-110853600	ZNF genes & repeats	Fetal Stomach	stomach
29	chr7:110853000-110853800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr7:110853000-110853800	Enhancers	Placenta	Placenta
31	chr7:110853000-110854000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr7:110853200-110853600	ZNF genes & repeats	Lung	lung
33	chr7:110853200-110853800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:110853200-110853800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr7:110853200-110853800	ZNF genes & repeats	Spleen	Spleen
36	chr7:110853400-110853600	Genic enhancers	Pancreas	Pancrea
37	chr7:110853400-110853800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr7:110853400-110853800	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr7:110853600-110854400	Weak transcription	Pancreas	Pancrea
40	chr7:110853600-110855000	Weak transcription	Fetal Stomach	stomach
41	chr7:110853600-110857000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:110853800-110854200	Weak transcription	Spleen	Spleen
43	chr7:110853800-110854600	Weak transcription	Placenta	Placenta
44	chr7:110853800-110854800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:110853800-110854800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr7:110853800-110857000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr7:110854000-110854200	Weak transcription	Lung	lung
48	chr7:110854000-110855600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr7:110854600-110854800	Enhancers	Placenta	Placenta
50	chr7:110854600-110855200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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